Health outcomes of children with Prader-Willi or Angelman syndromes: a European population-based multicentre study
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Background/aim: Prader-Willi syndrome (PWS) and Angelman syndrome (AS) are rare imprinting disorders caused by the aberrant expression of 15q11.2-q13 imprinted genes. Due to their rarity, data on health outcomes during infancy ar... ...
